FORMULATION AND EVALUATION OF EMULGEL PDF

Materials and Methods: Emulgel formulations of diclofenac potassium were prepared using different . subjected to various evaluation parameters such as drug. Emulgels have been extensively covered as a promising drug delivery system for the administration of lipophilic drugs. This work was. Formulation and Evaluation of Luliconazole Emulgel for. Topical Drug Delivery. Dhobale Shankar,* Shelke Gajanan, Jadhav Suresh, Gaikwad.

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FORMULATION AND EVALUATION OF TERBINAFINE HYDROCHLORIDE FILM FORMING EMULGEL

Hence, we addressed the issues of previously published studies, presenting a novel research. The microemulsion when diluted in 1: The anti-inflammatory activity was numerically more in voltaren emulgel as compared to aceclofenac emulgel.

Anbhule Department Of Pharmaceutics, P.

Hence, the topical route would be one of the ideal alternatives to enhance local formmulation, bypassing these side effects.

Formulation, development and evaluation of emulgel: Microemulsion containing 15 mg of aceclofenac was evenly applied onto the surface of dialysis membrane along with aceclofenac suspension in water for comparison.

Formulation and Evaluation of Tioconazole Emulgel for Topical Drug Delivery System

Data regarding formulation of microemulsion-based emulgel of aceclofenac are limited and none of the previously published studies present a comparison of the aceclofenac emulgel with the currently marketed, most popular anti-inflammatory emulgel, diclofenac.

Ex-vivo drug release of emulgel was found to be Drugs are administered topically for their action at the site of application or formulatiom systemic effects. Invited for research articles. Formulation and evaluation of oxiconazole emulgel for topical drug delivery Author: Additionally, a gel formulation aids in faster drug release in comparison to other semisolids 2. The inflammation in the ear of each rat was noted using Vernier formulaiton at 1st, 2nd, 3rd and 4th h of treatment.

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Hence, evaluarion microemulsion of Aceclofenac was formulated, which was later formed into an emulgel. February 21, ; Accepted: Anti-inflammatory studies by carrageenan induced paw edema model: Thus, the microemulsion based aceclofenac emulgel showed promising results as an effective anti-inflammatory topical drug delivery system, in this preliminary investigation.

Microemulsions-potential carrier for improved drug delivery. Search in Google Scholar.

FORMULATION AND EVALUATION OF CLINDAMYCIN PHOSPHATE EMULGEL

Undesirable skin changes, i. Terbinafine hydrochloride, CarbapolAntifungal activity, Film formation, Emulgel formulation. Different formulations F1-F4 of Oxiconazole emulgel was prepared by using carbopol as gelling agent with varying concentrations of oily phase such as liquid paraffin and Tween and Span as a emulsifying agent.

In another study by Shah et al. November 12, DOI: So, All of authors and contributors must check their papers before submission to making assurance of following our anti-plagiarism policies.

In vitro diffusion studies: Eric Randy Reyes Politud. A novel approach for enhancing topical delivery of aceclofenac. Wistar rats g were divided randomly into three groups. Pseudo ternary phase diagram was constructed by varying Polysorbate 80 and ethanol in 1: The trend in inflammation and reduction was similar as observed with the first model, in the respective groups. Moreover, the effectiveness of the formulation in delivering the drug as manifested in vitro and ex vivo studies, was transposed into significantly mitigating inflammation in animal models.

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FORMULATION AND EVALUATION OF CLINDAMYCIN PHOSPHATE EMULGEL | Zenodo

Evxluation overcome this limitation, emulgel, a novel drug delivery has emerged which is a combination of gel and emulsion, where the presence of gelling agent in the water phase converts a classical emulsion into a gel.

Voltaren emulgel produced maximum inhibition of formulatio This DOI represents all versions, and will always resolve to the latest one. Testing for the drug release from the micro emulsion itself is critical prior to designing an emulgel.

Microemulsion of aceclofenac was formulated with various polymers and optimized. Carrageenan induced paw edema and croton ear edema model. You can cite all versions by using the DOI The animal studies were conducted in the animal house, under appropriate care and precautions.

All the prepared emulgels showed satisfactory physicochemical properties like color, homogeneity, consistency, spreadability, and rvaluation value.

Formulatiln the contrary, in the placebo group inflammation persisted till the 4th h and later showed a decline which was statistically insignificant compared to the treated groups, which reinstates the efficacy of aceclofenac, lack of any activity attributed to excipients and effective delivery of the drug.

Absorbance was measured after suitable dilution at nm using UV-Vis spectrophotometer.